ITC CONTOUR EMBOLI, MODIFICATION

ITC CONTOUR EMBOLI, MODIFICATION is an FDA 510(k)-cleared medical device (K914866) manufactured by Interventional Therapeutics Corp.. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 8, 1993. Regulation: 8.